FDA product code NOB: Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Non-Sterile
NOB is the FDA product code for unit, ultraviolet sanitation/sterilization (for toothbrushes), non-sterile. It is a Class I device, regulated under 21 CFR 872.6855 and reviewed by the Dental panel. Devices under NOB reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Definition
manual toothbrush; see product code MCF
Classification
| Field | Value |
|---|---|
| Device name | Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Non-Sterile |
| Device class | Class I |
| Regulation | 21 CFR 872.6855 |
| Review panel | DE — Dental |
| Medical specialty | Dental |
| Premarket route | 510(k) exempt |
| GMP exempt | Yes |
Recalls for NOB devices
openFDA lists no recalls for product code NOB.
Frequently asked questions
What is FDA product code NOB?
NOB is the FDA product code for unit, ultraviolet sanitation/sterilization (for toothbrushes), non-sterile. It is a Class I device, regulated under 21 CFR 872.6855 and reviewed by the Dental panel.
What device class is NOB?
Class I, regulation 21 CFR 872.6855. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code NOB
- Run a recall and safety report across every NOB manufacturer
- Watch product code NOB for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
All Dental product codes · FDA product code lookup · 510(k) database search · 510(k) review times